Latest Innovation Jobs

ViiV Healthcare (GSK) Director, Clinical Pharmacology

This role involves leading clinical pharmacology strategy across HIV drug development programs, applying PK/PD and pharmacometric modeling to inform study design, regulatory decisions, and development pathways. The Director will mentor project leads, collaborate with cross-functional teams, and serve as a scientific expert in modeling and simulation to advance ViiV’s mission-driven HIV research from early to late-stage development.

GSK United States

Hybrid Permanent

ViiV Healthcare (GSK) Director, Clinical Pharmacology

This role involves providing scientific leadership in clinical pharmacology to shape drug development programs for HIV treatments. The Director will apply PK/PD, pharmacometrics, and model-informed drug development approaches to guide study design, regulatory strategy, and key decisions across early to late-stage development. Collaboration with cross-functional teams including clinical, regulatory, biostatistics, and CMC is central to advancing innovative therapies in a mission-driven environment focused on eradicating HIV.

GSK

Hybrid Permanent

ViiV Healthcare (GSK) Director, Clinical Pharmacology

This role involves leading clinical pharmacology strategy across HIV drug development programs, applying PK/PD, pharmacometrics, and modeling to inform study design, regulatory decisions, and development pathways. The Director will mentor project leads, collaborate with cross-functional teams, and serve as a scientific expert in model-informed drug development, contributing to breakthroughs in HIV treatment and prevention.

GSK

Hybrid Permanent

Principal Research Associate, Clinical Biomarker Laboratory, Flow Cytometry

This role involves generating and analyzing high-parameter flow cytometry data from clinical trial samples to support immunology research in a GCLP-compliant environment. The scientist will operate advanced spectral flow platforms like the Cytek Aurora, perform ex vivo immune functional assays, and ensure data integrity through rigorous documentation and compliance. Emphasis is placed on innovation through AI-enabled tools, assay development, and mentoring within a collaborative, regulated laboratory setting.

Moderna

Hybrid Permanent

Senior Research Associate, Bioanalytical & Molecular Assays

This role involves developing, qualifying, and validating molecular bioanalytical assays—such as qPCR, ddPCR, and gel electrophoresis—to support clinical-stage mRNA programs. The scientist will generate high-quality RNA quantitation data in compliance with GCLP standards, collaborate across clinical and laboratory teams, and contribute to regulatory documentation and sample management strategies. The position emphasizes innovation through digital tools and automation within a fast-paced, compliance-driven environment.

Moderna

Hybrid Permanent

Principal Scientist, Immunogenicity and Ligand Binding Assays

This role involves leading scientific strategy and execution for immunogenicity and ligand binding assay (LBA) bioanalysis within Moderna’s mRNA-LNP therapeutic development programs. The Principal Scientist will oversee regulated assay development, validation, and sample testing, ensuring compliance with GcLP, GLP, and regulatory standards. The position emphasizes cross-functional collaboration, data interpretation, and integration of emerging technologies, including AI-enabled analytics, to support clinical decision-making across the drug development lifecycle.

Moderna

Hybrid Permanent

Scientist, Clinical Biomarker Laboratory, Immuno-Assays - Cell Based

This role involves leading the development, qualification, and execution of complex cell-based immunoassays to support Moderna’s clinical trials across multiple therapeutic areas. The scientist will generate high-quality, regulatory-compliant data, serve as a subject matter expert, and collaborate with cross-functional teams and external partners. Emphasis is placed on assay innovation, scientific rigor, and integration of emerging technologies including digital and AI-enabled workflows.

Moderna

Hybrid Permanent

Senior Automation Engineer, Laboratory Automation & Biobanking

This role involves designing and optimizing automated laboratory workflows for biomarker testing and sample management within Moderna’s Clinical Biomarker Laboratory. The engineer will lead integration of advanced liquid handling systems, develop data pipelines, and ensure compliance with regulatory standards, while collaborating across digital, operations, and vendor teams to build scalable, AI-enhanced automation platforms.

Moderna

Hybrid Permanent

Research Associate, Assay Operations (Contractor)

This role involves executing high-throughput, multi-omics screening experiments using automated lab systems in 384- and 1536-well plates to generate data for drug discovery. The candidate will prioritize production workflows, maintain equipment and reagents, and contribute to process improvements through automation and optimization. Collaboration, proactive communication, and adherence to SOPs are essential in this fast-paced, mission-driven environment.

Recursion United Kingdom

On-site Contract

Associate Director, CMC Regulatory Affairs, International

This role involves developing and implementing CMC regulatory strategies for international submissions, providing guidance on regulatory CMC aspects, and leading regulatory discussions with health authorities. The candidate will also support the creation of CMC submission templates and offer interpretations of regulatory guidance documents, ensuring compliance and efficient delivery of high-quality regulatory documentation.

Moderna

On-site Permanent

Senior Director / Director, Non-Clinical Safety Project Specialist

This role leads non-clinical safety strategy across drug discovery and development, integrating scientific data to inform project decisions, regulatory submissions, and risk assessment. The specialist provides expert guidance on safety profiling, candidate selection, and translational planning, while mentoring teams and shaping regulatory narratives. They work cross-functionally to ensure robust safety evaluation for small molecules and biologics through clinical and post-market stages.

GSK £224,400 – £374,000 pa

On-site Permanent

Senior Director / Director, Non-Clinical Safety Project Specialist

This role leads non-clinical safety strategy across drug discovery and development, integrating scientific data to inform project decisions, regulatory submissions, and risk assessment. The position involves mentoring teams, shaping translational plans, and providing expert input on safety profiling and candidate selection. It plays a key part in regulatory strategy and cross-functional leadership within a global biopharma environment.

GSK £224,400 – £374,000 pa

Hybrid Permanent

Associate Director- Diagnostics Precision Medicine

This role involves leading diagnostic strategies in oncology drug development, focusing on end-to-end execution of biomarker-driven clinical trials. The individual will oversee assay development and validation, manage cross-functional teams, and ensure regulatory compliance across global studies. Collaboration with IVD partners and integration of advanced diagnostic technologies like NGS and liquid biopsy are key components of the position.

GSK United States £150,975 – £251,625 pa

Hybrid Permanent

Director, Global RWE-HO, Oncology

Leads the planning, design, and execution of real-world evidence (RWE) and health outcomes studies to support oncology assets across the product lifecycle. Collaborates with cross-functional teams to generate robust evidence for regulatory, reimbursement, and market access decisions. Focuses on translating clinical and economic value into impactful data for payers, providers, and patients.

GSK United States

Hybrid Permanent

Director, Global RWE-HO, Oncology

This role involves leading the design and execution of real-world evidence (RWE) and health outcomes studies to support oncology assets across their lifecycle. The Director will develop robust data generation plans, align evidence with regulatory and payer requirements, and collaborate with cross-functional teams and external experts to ensure impactful evidence for market access and patient outcomes. The position plays a strategic role in shaping value propositions through scientifically credible research in a global, matrix environment.

GSK

Hybrid Permanent